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9-(4-Chloro-6-phenyl-1,3,5-triazin-2-yl)-9H-carbazole

  • CAS No. 1268244-56-9

  • Cat. No. CS-0135879
  • Purity≥97%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

9-(4-Chloro-6-phenyl-1,3,5-triazin-2-yl)-9H-carbazole|CS-0135879

Structure of 1268244-56-9

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General Information

  • CAS No. 1268244-56-9
  • Cat. No. CS-0135879
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₁H₁₃ClN₄
  • Molecular Weight 356.81
  • Synonym(s) 9-[3-(4-Chloro-6-phenyl-[1,3,5]triazin-2-yl)-phenyl]-9H-carbazole
  • SMILES ClC1=NC(C2=CC=CC=C2)=NC(N3C4=C(C5=C3C=CC=C5)C=CC=C4)=N1

Description

9-(4-Chloro-6-phenyl-1,3,5-triazin-2-yl)-9H-carbazole is a sterically hindered triazine-functionalized carbazole bearing a chloro substituent at the 4-position and a phenyl group at the 6-position. This configuration enhances electronic coupling and stability in photoredox applications. The molecule integrates readily into conjugated systems for use in organic semiconductors and light-harvesting materials.

Application

9-(4-Chloro-6-phenyl-1,3,5-triazin-2-yl)-9H-carbazole serves as a versatile building block in the synthesis of functionalized triazine-linked heterocycles. Its chloro-substituted triazine moiety enables efficient coupling reactions with nucleophiles, including amines and alcohols, under mild conditions. The carbazole core provides structural rigidity and electronic conjugation, enhancing utility in materials chemistry and medicinal scaffolds. Bench-stable and readily purified by chromatography, it facilitates scalable synthesis of advanced intermediates.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   43.6
  • LogP   5.2891
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   2

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